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KCNJ10 - potassium inwardly rectifying channel subfamily J member 10
- Synonym(s) : Kir1.2, Kir4.1
- Previous symbols and names : potassium inwardly-rectifying channel, subfamily J, member 10
- Type : gene with protein product
- Chromosomal location : 1q23.2
- OMIM: 602208
- HGNC: 6256
- UniProtKB: P78508
- Genatlas: KCNJ10
- Ensembl: ENSG00000177807
- IUPHAR-DB: 438
- Reactome: P78508
- LOVD: KCNJ10
Diseases list
- Disease-causing germline mutation(s) in EAST syndrome
ORPHA:199343 
- Disease-causing germline mutation(s) in Pendred syndrome
ORPHA:705
: AssessedGene included in a panel of genes performed as part of a diagnostic test
Additional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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